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Mucin Hypersecreting Intraductal Papillary Neoplasm of the Pancreas

Mucin Hypersecreting Intraductal Papillary Neoplasm is a rare neoplasm that arises from ductal epithelial cells. This entity is distinct from the more commonly known Mucinous Cystadenoma or Mucinous Cystadenocarcinoma. Despite this distinction, it has been erroneously categorized with these more com...

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Detalles Bibliográficos
Autores principales: Kim, Anthony W., Ryan, Anna, Millikan, Keith W., Doolas, Alexander
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423964/
https://www.ncbi.nlm.nih.gov/pubmed/10371063
http://dx.doi.org/10.1155/1999/81649
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author Kim, Anthony W.
Ryan, Anna
Millikan, Keith W.
Doolas, Alexander
author_facet Kim, Anthony W.
Ryan, Anna
Millikan, Keith W.
Doolas, Alexander
author_sort Kim, Anthony W.
collection PubMed
description Mucin Hypersecreting Intraductal Papillary Neoplasm is a rare neoplasm that arises from ductal epithelial cells. This entity is distinct from the more commonly known Mucinous Cystadenoma or Mucinous Cystadenocarcinoma. Despite this distinction, it has been erroneously categorized with these more common cystic neoplasms. Characteristic clinical presentation, radiographic, and endoscopic findings help distinguish this neoplasm from the cystadenomas and cystadenocarcinomas. Histopathologic identification is not crucial to the preoperative diagnosis. This neoplasm is considered to represent a premalignant condition and, therefore, surgical resection is warranted. Prognosis, following resection, is felt to be curative for the majority of patients. We present two cases of Mucin Hypersecreting Intraductal Papillary Neoplasm and discuss their diagnosis and surgical therapy.
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spelling pubmed-24239642008-07-08 Mucin Hypersecreting Intraductal Papillary Neoplasm of the Pancreas Kim, Anthony W. Ryan, Anna Millikan, Keith W. Doolas, Alexander HPB Surg Research Article Mucin Hypersecreting Intraductal Papillary Neoplasm is a rare neoplasm that arises from ductal epithelial cells. This entity is distinct from the more commonly known Mucinous Cystadenoma or Mucinous Cystadenocarcinoma. Despite this distinction, it has been erroneously categorized with these more common cystic neoplasms. Characteristic clinical presentation, radiographic, and endoscopic findings help distinguish this neoplasm from the cystadenomas and cystadenocarcinomas. Histopathologic identification is not crucial to the preoperative diagnosis. This neoplasm is considered to represent a premalignant condition and, therefore, surgical resection is warranted. Prognosis, following resection, is felt to be curative for the majority of patients. We present two cases of Mucin Hypersecreting Intraductal Papillary Neoplasm and discuss their diagnosis and surgical therapy. Hindawi Publishing Corporation 1999-04 /pmc/articles/PMC2423964/ /pubmed/10371063 http://dx.doi.org/10.1155/1999/81649 Text en Copyright © 1999 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kim, Anthony W.
Ryan, Anna
Millikan, Keith W.
Doolas, Alexander
Mucin Hypersecreting Intraductal Papillary Neoplasm of the Pancreas
title Mucin Hypersecreting Intraductal Papillary Neoplasm of the Pancreas
title_full Mucin Hypersecreting Intraductal Papillary Neoplasm of the Pancreas
title_fullStr Mucin Hypersecreting Intraductal Papillary Neoplasm of the Pancreas
title_full_unstemmed Mucin Hypersecreting Intraductal Papillary Neoplasm of the Pancreas
title_short Mucin Hypersecreting Intraductal Papillary Neoplasm of the Pancreas
title_sort mucin hypersecreting intraductal papillary neoplasm of the pancreas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423964/
https://www.ncbi.nlm.nih.gov/pubmed/10371063
http://dx.doi.org/10.1155/1999/81649
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